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厌氧甘油-3-磷酸脱氢酶:大肠杆菌glpA基因的克隆与表达及glpA产物的鉴定

The anaerobic sn-glycerol-3-phosphate dehydrogenase: cloning and expression of the glpA gene of Escherichia coli and identification of the glpA products.

作者信息

Schryvers A, Weiner J H

出版信息

Can J Biochem. 1982 Mar;60(3):224-31. doi: 10.1139/o82-027.

Abstract

The expression of recombinant plasmids carrying the glpA gene (anaerobic glycerol-3-phosphate dehydrogenase) and the closely linked glpT gene (glycerol 3-phosphate transport) were studied under aerobic and anaerobic conditions. When the pattern of expression of enzymatic activity in different strains was compared with sodium dodecyl sulphate - polyacrylamide gel electrophoresis (SDS-PAGE) analysis from the same cells the glpA products were identified. Two polypeptides of 62 000 and 43 000 relative mass correlated with enzymatic activity. Five recombinant plasmids that contained one or both of the glpT of glpA genes were isolated and subjected to restriction endonuclease cleavage analysis. The regions of overlap from the inserts in these plasmids allowed definition of the regions of DNA containing the glpT and glpA genes. SDS-PAGE analysis revealed a partial product of the glpA locus from one plasmid, pLC42-17, which allowed more precise definition of the glpA locus on the physical DNA map and prediction of the direction of transcription.

摘要

对携带glpA基因(厌氧甘油-3-磷酸脱氢酶)和紧密连锁的glpT基因(甘油3-磷酸转运蛋白)的重组质粒在需氧和厌氧条件下的表达进行了研究。当将不同菌株中酶活性的表达模式与来自相同细胞的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分析进行比较时,鉴定出了glpA产物。两种相对分子质量分别为62000和43000的多肽与酶活性相关。分离出了五个含有glpA基因的glpT之一或两者的重组质粒,并对其进行了限制性内切酶切割分析。这些质粒中插入片段的重叠区域使得能够确定包含glpT和glpA基因的DNA区域。SDS-PAGE分析揭示了来自一个质粒pLC42-17的glpA基因座的部分产物,这使得能够在物理DNA图谱上更精确地确定glpA基因座,并预测转录方向。

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